ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825612677
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376679
ClinVar RCV Id:
RCV000421406
RCV000422095
RCV000424159
RCV000427021
RCV000426404
RCV000428833
RCV000431660
RCV000434430
RCV000437297
RCV000439053
RCV000439742
RCV000443298
RCV000443877
RCV000444003
RCV000633347
RCV002338982
RCV004022250
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119588.1:p.Tyr31Asn
CA16603093
NM_001126116.1:c.91T>A